Evidence map›Paper›PMID 27538453›Full record

ArticleScientific reports2016

Spherical nucleic acid targeting microRNA-99b enhances intestinal MFG-E8 gene expression and restores enterocyte migration in lipopolysaccharide-induced septic mice.

Xiao Wang, Liangliang Hao, Heng-Fu Bu, Alexander W Scott, Ke Tian, Fangyi Liu, Isabelle G De Plaen, Yulan Liu, Chad A Mirkin, Xiao-Di Tan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Review
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  10. Conjugation of Nucleic Acids and Drugs to Gold Nanoparticles.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  11. Article
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  13. Review
  14. Article
  15. Article
  16. Spherical Nucleic Acid Nanoparticles: Therapeutic Potential.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2018
    Review
  17. Article
  18. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Xiao WangCenter for Intestinal and Liver Inflammation Research, Stanley Manne Children's Research Institute, Ann &Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.
Liangliang HaoDepartment of Chemistry and the International Institute for Nanotechnology, Northwestern University, Evanston, IL 60208, USA.
Heng-Fu BuCenter for Intestinal and Liver Inflammation Research, Stanley Manne Children's Research Institute, Ann &Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.
Alexander W ScottDepartment of Biomedical Engineering, Northwestern University, Evanston, IL 60208, USA.
Ke TianCenter for Intestinal and Liver Inflammation Research, Stanley Manne Children's Research Institute, Ann &Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.
Fangyi LiuCenter for Intestinal and Liver Inflammation Research, Stanley Manne Children's Research Institute, Ann &Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.
Isabelle G De PlaenCenter for Intestinal and Liver Inflammation Research, Stanley Manne Children's Research Institute, Ann &Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.
Yulan LiuDepartment of Gastroenterology, Peking University People's Hospital, Beijing 100044, P. R. China.
Chad A MirkinDepartment of Chemistry and the International Institute for Nanotechnology, Northwestern University, Evanston, IL 60208, USA.
Xiao-Di TanCenter for Intestinal and Liver Inflammation Research, Stanley Manne Children's Research Institute, Ann &Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.
Northwestern University · USLurie Children's Hospital · USPeking University · CN

Funding

Project 3: Spherical Nucleic Acids as Immunotherapeutic Agents for Prostate CancerU54CA199091 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MIRKIN, CHAD A. · 2015 to 2019
$11.7M
Theranostic Magnetic Nanostructures for the Molecular Imaging of CancerU54CA151880 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WOLOSCHAK, GAYLE E. · 2010 to 2014
$11.5M
Preservation of mucosal barrier in surgical diseasesR01DK064240 · NIDDK · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI TAN, XIAO-DI · 2004 to 2014
$3.0M
Cell-specific role of NF-KB in necrotizing enterocolitisR01HD060876 · NICHD · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI DE PLAEN, ISABELLE G · 2010 to 2014
$1.5M
MFG-E8 and progression of alcohol-induced tissue injuryR21AA020494 · NIAAA · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI TAN, XIAO-DI · 2011 to 2012
$386k
Mechanisms of trauma and hemorrhage-induced impairment of innate immunityI01BX001690 · VA · JESSE BROWN VA MEDICAL CENTER · PI TAN, XIAO-DI · 2013 to 2016
–
BLRD VA I01 BX001690Howard Hughes Medical InstituteNCI NIH HHS U54 CA151880NCI NIH HHS U54 CA199091NIAAA NIH HHS R21 AA020494NICHD NIH HHS R01 HD060876NIDDK NIH HHS R01 DK064240
6 · The paper itself

Abstract

Milk fat globule-EGF factor 8 (MFG-E8) maintains the intestinal homeostasis by enhancing enterocyte migration and attenuating inflammation. We previously reported that sepsis is associated with down-regulation of intestinal MFG-E8 and impairment of enterocyte migration. Here, we showed that impairment of intestinal epithelial cell migration occurred in lipopolysaccharide (LPS)-induced septic mice. Treatment of RAW264.7 cells (a murine macrophage-like cell line) with LPS increased expression of miR-99b, a microRNA that is predicted to target mouse MFG-E8 3'UTR. Using a luciferase assay, we showed that miR-99b mimic suppressed the activity of a reporter containing MFG-E8 3'UTR. This suggests the role of miR-99b in inhibition of MFG-E8 gene expression. In addition, we developed an anti-miR99b spherical nucleic acid nanoparticle conjugate (SNA-NC(anti-miR99b)). Treatment of both naïve and LPS-challenged cells with SNA-NC(anti-miR99b) enhanced MFG-E8 expression in the cells. Administration of SNA-NC(anti-miR99b) rescued intestinal MFG-E8 expression in LPS-induced septic mice and attenuated LPS inhibitory effects on intestinal epithelial cell migration along the crypt-villus axis. Collectively, our study suggests that LPS represses MFG-E8 expression and disrupts enterocyte migration via a miR-99b dependent mechanism. Furthermore, this work shows that SNA-NC(anti-miR99b) is a novel nanoparticle-conjugate capable of rescuing MFG-E8 gene expression and maintaining intestinal epithelial homeostasis in sepsis.

Indexed as

AnimalsAntigens, SurfaceCell MovementEnterocytesGene Expression RegulationGene TargetingLipopolysaccharidesMaleMiceMicroRNAsMilk ProteinsRAW 264.7 CellsSepsisAntigens, SurfaceLipopolysaccharidesMfge8 protein, mouseMicroRNAsMilk ProteinsMirn99 microRNA, mouse

Identifiers

PMID27538453
PMCPMC4990839
OpenAlexW2509086526

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.